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A Phase 2 Study of TAS-303 in Female Patients With Stress Urinary Incontinence

Stress Urinary Incontinence Clinical Trial

Official title:
A Phase 2, Randomized, Placebo-controlled, Double-blind Study of TAS-303 in Female Patients With Stress Urinary Incontinence

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of TAS-303 in female patients with stress urinary incontinence.

Clinical Trial Description

The main purpose of this study is to assess the efficacy of TAS-303 in female patients with stress urinary incontinence (SUI) compared with placebo as measured by the percent change in the average SUI episode frequency per 24 hours from baseline at week 12. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04512053
Study type Interventional
Source Taiho Pharmaceutical Co., Ltd.
Contact
Status Completed
Phase Phase 2
Start date September 4, 2020
Completion date December 22, 2021
View Details
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